This half-day workshop is designed to provide the opportunity to explore the consent process in more depth covering Good Clinical Practice (GCP) and the requirements of the UK Policy Framework for Health and Social Care Research, EU Directives and UK Regulations, which cover NIHR Portfolio studies and clinical trials conducted within the NHS. The workshop also covers practical issues and some scenarios to enhance learning.
Expected Learning Outcomes
Following the course, participants will have a demonstrable understanding of the background and practical implications of the informed consent process. This understanding is intended to be a foundation for action about translating principles into practice and give participants the confidence to take a proactive role in the consent process back in the workplace.
NB: This course would be useful to anyone involved in the consent process, not just training for those actively receiving consent in practice.
You will have to have an NIHR Learn account set up in order to attend a session.
The online courses are interactive sessions and to get the most from it, you will need to be able to engage in group activity and discussion. To be able to participate fully, you will need to have access to the following:
- A quiet room or environment where you will not be disturbed by, or disturb others
We also strongly recommend that you download and install the Zoom application where possible. Whilst these sessions can be joined using a web browser this can create functional limitations that may reduce your experience.